Siemens Healthcare Diagnostics, Inc. 2025-01-01 Health serious FDA
Health · FDA · Recall #FDA-Z-0767-2025
Magnesium Flex reagent cartridge, 360 tests, Catalog Number: K3057; Siemens Material… Recall
Issued January 1, 2025 · Siemens Healthcare Diagnostics, Inc.
In January 2025, Siemens Healthcare Diagnostics, Inc. recalled the Magnesium Flex reagent cartridge, 360 tests, Catalog Number: K3057; Siemens Material…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Siemens Healthcare Diagnostics is recalling two lots of their Dimension Vista¿ Total Magnesium (MG) Flex Reagent Cartridges (lots 24057BB and 24064BC) due to the potential for falsely low measurements of magnesium in plasma. Because the error is intermittent, existing quality control procedures may not recognize that a patients results are incorrect, and the results may be reported out
What you should do
- 1 Stop using Magnesium Flex reagent cartridge, 360 tests, Catalog Number: K3057; Siemens Material… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Siemens Healthcare Diagnostics, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Siemens Healthcare Diagnostics, Inc.
- Category
- Health
- Recall date
- January 1, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, Denmark, France, Germany, Italy, Slovenia,
- Recall number
- FDA-Z-0767-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Siemens Healthcare Diagnostics, Inc. has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.